BEUDAMED
    3 results · 35ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 9, 2014

    SL PLUS

    FDA Adverse Event
    Injury ·SMITH & NEPHEW-SWITZERLAND·Product code KWY·December 3, 2012

    DURACON CRUC BEADED B/P M2

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS LIMERICK·Product code MBH·September 30, 2010